Literature DB >> 31655771

Low-Renin Hypertension.

Shobana Athimulam1, Natalia Lazik2, Irina Bancos3.   

Abstract

Low-renin hypertension affects 30% of hypertensive patients. Primary hyperaldosteronism presents with low renin and aldosterone excess. Low-renin, low-aldosterone hypertension represents a wide spectrum of disorders that includes essential low-renin hypertension, hereditary forms of hypertension, and hypertension secondary to endogenous or exogenous factors. This review addresses the different conditions that present with low-renin hypertension, discussing an appropriate diagnostic approach and highlighting the genetic subtypes within familial forms.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Apparent mineralocorticoid excess syndrome; CYP11B1 and CYP17 deficiency; Glucocorticoid-resistance syndrome; Gordon syndrome; Liddle syndrome; Low-renin hypertension; Mineralocorticoid receptor– activating mutation; Primary aldosteronism

Mesh:

Substances:

Year:  2019        PMID: 31655771     DOI: 10.1016/j.ecl.2019.08.003

Source DB:  PubMed          Journal:  Endocrinol Metab Clin North Am        ISSN: 0889-8529            Impact factor:   4.741


  4 in total

1.  Pediatric Liddle Syndrome Caused by a Novel SCNN1G Variant in a Chinese Family and Characterized by Early-Onset Hypertension.

Authors:  Peng Fan; Xiao-Cheng Pan; Di Zhang; Kun-Qi Yang; Ying Zhang; Tao Tian; Fang Luo; Wen-Jun Ma; Ya-Xin Liu; Lin-Ping Wang; Hui-Min Zhang; Lei Song; Jun Cai; Xian-Liang Zhou
Journal:  Am J Hypertens       Date:  2020-07-18       Impact factor: 2.689

2.  Positive Association Between Plasma Aldosterone Concentration and White Matter Lesions in Patients With Hypertension.

Authors:  Yujuan Yuan; Nanfang Li; Yan Liu; Qing Zhu; Mulalibieke Heizhati; Weiwei Zhang; Xiaoguang Yao; Deilian Zhang; Qin Luo; Menghui Wang; Guijuan Chang; Mei Cao; Keming Zhou; Lei Wang; Junli Hu; Nuerguli Maimaiti
Journal:  Front Endocrinol (Lausanne)       Date:  2021-11-18       Impact factor: 5.555

3.  A Novel Homozygous KLHL3 Mutation as a Cause of Autosomal Recessive Pseudohypoaldosteronism Type II Diagnosed Late in Life.

Authors:  Annika Etges; Nicole Hellmig; Gudrun Walenda; Bassam G Haddad; Jan-Philipp Machtens; Thomas Morosan; Lars Christian Rump; Ute I Scholl
Journal:  Nephron       Date:  2022-01-28       Impact factor: 3.457

4.  Editorial: Insights in renal endocrinology: 2021.

Authors:  Nehal M Elsherbiny; Eman Said
Journal:  Front Endocrinol (Lausanne)       Date:  2022-09-20       Impact factor: 6.055

  4 in total

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